Multi-carotenoids compositions and uses therefor

ABSTRACT

Methods for ameliorating the effects of benign prostate hyperplasia (BPH)-related lower urinary tract symptoms (LUTS) in men, comprising orally administering an effective amount of multi-carotenoids compositions. Multi-carotenoids composition for oral administration comprising about 71% by weight, of a tomato extract containing therein about 2% to 10% by weight of lycopene, about 0.25% to 2% by weight of phytoene, and about 0.2% to 2% by weight of phytofluene, and about 29% by weight, of a suitable encapsulating matrix. A suitable encapsulating matrix is an edible oil exemplified by soya oil, pumpkin seed oil, grape-seed oil and the like. The tomato extract may additionally comprise one or more of at least one carotene selected from the group comprising β-carotene, γ-carotene, and δ-carotene, a phytosterol, a tocopheral and a phospholipid. Use of multi-carotenoids compositions for the treatment of urinary tract malfunctions including benign prostate hyperplasia and lower urinary tract symptoms.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation-in-part application of co-pendingU.S. patent application Ser. No. 11/695,354 filed Apr. 2, 2007, whichclaims priority from Taiwanese Patent Application Serial No. 095111722,filed Apr. 3, 2006, currently pending.

TECHNICAL FIELD

This invention relates to compositions comprising a plurality ofcarotenoid compounds and methods for oral administration of carotenoidscompositions for ameliorating the effects of aging-related urinaryimpairments and malfunctions in men. More particularly, the presentinvention is directed to compositions comprising at least lycopene,phytoene and phytofluene, for oral administration as a nutritionalsupplement and/or a botanical drug. The present invention also relatesto methods for use of said compositions disclosed herein.

BACKGROUND OF THE INVENTION

Lycopene and its precursor phytofluene are carotenoids commonly found intomatoes and are the predominant sources of the bright red colorassociated with tomatoes. Phytoene is a precursor to phytofluene,lycopene and other carotenoids, and is also found in high concentrationsin tomatoes. Lycopene is generally present in the plasma of the humanbody; the serum concentrations of lycopene are typically about 2.5 timeshigher than those of α-carotene and 7.5 times greater than those ofβ-carotene. Carotenoids are known to have antioxidant properties andconsequently, provide numerous beneficial health effects includingreducing the potential risks of cardiovascular diseases, cancers, andslowing and/or reversing the degenerative effects of aging on varioushuman physiological activities.

Carotenoids are a group of pigments that are characterized by the colorincluding and ranging from yellow to red. Carotenoids are commonlyproduced by a wide variety of plant materials and most commonlyassociated with plants such as tomatoes, carrots and peppers.

Benign prostates hyperplasia (also called BPH) and prostate cancer areaging-related conditions that affect prostate gland physiology andimpair urinary function in men. As many men age, their prostate glandsslowly enlarge causing (a) obstructive symptoms exemplified by weakand/or intermittent urinary streams, a sense of residual urine in thebladder after voiding, and dribbling or leakage at the end of urination,and/or (b) irritative symptoms as exemplified by urgency of micturation,increased frequency of urination, and uracratia. Obstructive andirritative urinary symptoms are commonly referred to as lower urinarytract symptoms (LUTS). The current treatments of prostate cancer, BPHand LUTS symptoms consist of drug therapies and major surgery. The twoprimary drug classes used are alpha-blockers and 5-alpha-reductaseinhibitors, which should be taken for life in order to get thepersistent efficacy. When surgery is considered, the results are usuallypositive, but there are risks associated with such surgical operations.

SUMMARY OF THE INVENTION

Embodiments of the present invention relate to multi-carotenoidscompositions for oral administration as nutritional supplements orbotanical drugs, wherein the compositions comprise at least lycopene,phytoene, phytofluene components, and a suitable carrier.

According to one embodiment, there are provided methods for oraladministration of multi-carotenoids compositions for ameliorating theeffects of aging-related urinary impairments and malfunctions in men.Such urinary impairments and malfunctions are exemplified by benignprostatic hyperplasia and lower urinary tract symptoms such asobstructive symptoms and irritative symptoms, and the like. Themulti-carotenoids compositions for oral administration comprise at leastlycopene, phytoene, phytofluene components, and a suitable carrier.

Another embodiment relates to methods for ameliorating the effects ofaging-related urinary tract malfunctions in men, where the urinary tractmalfunctions comprise the group of benign prostate hyperplasia and lowerurinary tract symptoms, and the method comprises orally administratingan effective amount of a composition comprising:

a tomato extract comprising about 2% to 10% by weight of lycopene, about0.25% to 2% by weight of phytoene, and about 0.2% to 2% by weight ofphytofluene;

an edible oil; and

a suitable carrier.

In one embodiment, the multi-carotenoids compositions are nutritionalsupplements and/or botanical drugs.

According to one aspect, the lycopene, phytoene, and phytofluenecomponents of the multi-carotenoid compositions are preferably naturallyoccurring and are preferably extracted from tomatoes as pulp. The tomatopulp is further processed into oleoresins, beadlets, dry powdermaterials, paste and combinations thereof.

In one embodiment, the tomato extract and edible oil are furtherprocessed into soft-gel capsules, or alternatively, in “hard” capsules,or optionally, configured into tablets, or if so desired, into sachetpackets, beverages, and combinations thereof.

According to another aspect, the tomato extracts comprising themulti-carotenoids compositions of the present invention may additionallycontain one or more of β-carotene, γ- carotene, and δ-carotene, aphytosterol, a tocopheral and a phospholipid.

In one embodiment, the multi-carotenoids compositions comprise lycopene,phytoene, phytofluene, and vitamin E components with trace amounts ofβ-carotene, γ-carotene, and δ-carotene, within a tomato oil matrix. Thismatrix is encased in a soft gel capsule. The composition mayadditionally comprise an edible oil exemplified by soya oil, pumpkinseed oil, grapeseed oil and the like. Alternatively, the matrix isencased in a hard capsule.

A further embodiment relates to the use of multi-carotenoidscompositions for the treatment of urinary tract malfunctions comprisingthe group of benign prostate hyperplasia and lower urinary tractsymptoms. The composition comprises at least lycopene, phytoene, andphytofluene; and a suitable carrier. In another aspect, the compositioncomprises: a tomato extract comprising about 2% to 10% by weight oflycopene, about 0.25% to 2% by weight of phytoene, and about 0.2% to 2%by weight of phytofluene; an edible oil; and a suitable carrier. In afurther aspect, the composition comprises: a tomato extract comprisingabout 4% to 7% by weight of lycopene, about 0.4% to 0.7% by weight ofphytoene; about 0.3% to 0.6% by weight of phytofluene, about 1% to 3% byweight of a tocopherol, about 1% to 2% by weight of a β-carotene, about0.3% to 0.6% by weight of a phytosterol, about 5% to 10% by weight of aphospholipid; an edible oil; and a suitable carrier.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the present invention will be described with reference tothe following drawings:

FIG. 1 is a lycopene isomer;

FIG. 2 is a phytoene isomer; and

FIG. 3 is a phytofluene isomer.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides stable multi-carotenoids compositionsuseful for oral administration as nutritional supplements and/orbotanical drugs, wherein the compositions comprise at least lycopene,phytoene, phytofluene components contained within an extract producedfrom tomato fruits. Suitable tomato fruits are produced bynon-genetically engineered plants, and preferably contain highconcentrations of lycopene. The compositions are preferably encased in asoft gel capsule and may additionally comprise an edible oil exemplifiedby soya oil, pumpkin seed oil, grapeseed oil and the like.

Botanical drugs are generally understood to be products intended for usein the diagnosis, cure, mitigation, treatment or prevention of diseasein humans. Botanical drug products typically include vegetablematerials, which may include plant materials, algae, macroscopic fungi,or combinations thereof.

The lycopene, phytoene and phytofluene components are preferablyprocessed from tomato fruits into extracts. The components may beconcentrated by removing water from the extracts thereby producingthickened pulps that contain therein the lycopene, phytoene andphytofluene components, and additionally comprise β-carotene,γ-carotene, δ-carotene, vitamin E, a plurality of phytosterols andphospholipids. The thickened pulps may be further suitably processedinto oleoresin-based emulsions. The oleoresins may be encapsulatedwithin soft gel capsules comprising soya oil or alternatively, pumpkinseed oil, grapeseed oil or combinations thereof. The tomato extracts maybe optionally formulated into beadlets that may be packaged if sodesired in sachet packets, or alternatively, dried and processed intopowders and pastes that may be optionally encapsulated or alternatively,tabletted. Alternatively, tomato extracts may be formulated intobeverages.

Lycopene in its natural state, contained within for example a tomato,does not have the same benefits as when it is extracted and formulatedinto a nutritional supplement or and/botanical drug.

The synergistic effect of the combination of carotenoids and otherbioactive compounds such as vitamin C, vitamin E and flavonoids is knownin the art to provide improved health benefits. In one embodiment, themulti-carotenoids compositions include naturally extracted carotenoidsthat have complex chemical structures. The multi-carotenoidscompositions contain lycopene, as well as tocopherols, phytoene,phytofluene, beta-carotene and other bioactive phytochemicals. Thesynergistic effect of lycopene in combination with phytoene andphytofluene was compared to the effect of the administration of the samecarotenoids alone. For example, on administration of a low concentrationof lycopene in combination with phytoene and phytofluene, a synergisticinhibition of cancer cell growth was evident (data not shown) oncomparison to the administration of lycopene alone.

In one embodiment, the multi-carotenoids composition is administeredorally on a regular basis. In another embodiment, the multi-carotenoidscomposition is administered weekly. In an alternative embodiment, themulti-carotenoids composition is administered daily. In a furtherembodiment, the multi-carotenoids composition is administered everyother day. In a further embodiment, the multi-carotenoids composition isadministered every third day.

In one embodiment, the multi-carotenoids composition of the presentinvention is a soft gel capsule that is orally administered andcomprises about: (a) 71% by weight of a tomato extract containing about2% to 10% by weight of lycopene, 0.25% to 2% by weight of phytoene, 0.2%to 2% by weight of phytofluene, trace amounts of β-carotene, γ-carotene,δ-carotene, vitamin E, phytosterols and phospholipids, and (b) 29%weight of a suitable encapsulating matrix exemplified by soya oil orpumpkin seed oil. One exemplary multi-carotenoids composition is a softgel capsule weighing about 350 mg and comprising firstly, about 250 mgof a tomato oleoresin containing: (a) about 15 mg of lycopene, (b) about1.5 mg of phytoene, (c) about 1.25 mg of phytofluene, (d) about 0.5 mgof vitamin E, (e) about 5 mg of β-carotene, (f) about 1.5 mg of aphytosterol, and (g) about 25 mg of a phospholipid, and secondly, about100 mg of soya oil or alternatively, about 100 mg of pumpkin seed oiland the like. The soft gel capsule may be a nutritional supplementand/or a botanical drug.

In one embodiment, the multi-carotenoids composition of the presentinvention comprises at least one of an isomer of lycopene as exemplifiedin FIG. 1, an isomer of phytoene as exemplified in FIG. 2, and an isomerof phytofluene as exemplified in FIG. 3. Lycopene is an acyclic isomerof β-carotene. It is a 40 carbon atom, open chain polyisoprenoid with 11conjugated double bonds and has the molecular formula C₄₀H₅₆.All-(E)-lycopene is the predominant geometric isomer found in plants.(Z)-isomers of lycopene are also found in nature, including (5Z)-,(9Z)-, (13Z)- and (15Z)- isomers. The structural formula of a preferredlycopene isomer is represented in FIG. 1. Phytoene is an intermediate inthe biosynthesis of carotenoids and has the molecular formula C₄₀H₆₄ .All-trans-phytoene is the predominant geometric isomer found in plants.The structural formula of a preferred phytoene isomer is represented inFIG. 2. Phytofluene is a product of carotenoid biosynthesis and has themolecular C₄₀H₆₂. All-trans-phytofluene is the predominant geometricisomer found in plants. The structural formula of a preferredphytofluene isomer is represented in FIG. 3.

In one embodiment, the multi-carotenoids composition may be administeredfor the treatment of aging-related urinary impairments and malfunctionsin men. These aging-related urinary impairments and malfunctions in menare exemplified by benign prostatic hyperplasia, prostate cancer, lowerurinary tract symptoms such as obstructive symptoms and irritativesymptoms, and the like.

EXAMPLE 1 Effects of a Multi-Carotenoids Composition on PatientsExhibiting Urinary Impairments

A 12-week phase II clinical study was initiated with a group of 74 malesdivided into two sub-groups of 37 individuals each, to assess theeffects of an exemplary capsule formulation of the multi-carotenoidscomposition of the present invention. More specifically, the clinicalstudy evaluated the potential effects of administration of amulti-carotenoids composition on serum PSA levels and LUTS. Inparticular, the study evaluated the effects of a multi-carotenoidscomposition administration on benign prostate hypertrophy (BPH). Twelveindividuals were subsequently withdrawn from the study due to ascreening failure. The remaining 63 subjects were divided into: (a) afirst study group of 29 subjects who received a daily oral dose of one350-mg capsule of the exemplary capsule of the present invention therebyproviding a daily nutritional supplement of 15 mg of lycopene, and (b) asecond study group of 32 subjects who received a daily oral dose of two350-mg capsules of the present invention thereby providing a dailynutritional supplement of 30 mg of lycopene, on selected clinicalparameters associated with prostate and urinary system health. Theinclusion criteria for the trial were male subjects over 40 years of agewith no prior history or indicators of prostate and/or other cancers,the subjects' prostate specific antigen (PSA) levels were between 2.5and 20.0 ng/ml, and their renal and liver functions were within normalranges. The exclusion criteria were individuals with fluctuating PSAlevels, recent medical histories of urinary tract infection,prostatitis, acute urinary retention, individuals with known allergicreactions to carotenoids, individuals taking medications that may alterserum PSA levels as exemplified by 5-α reductase inhibitors, steroids orhormonal agents, and medications for lower urinary tract infections.

The trial followed a general protocol of, first, screening, evaluationand selection of the individuals for participating in the trial. Second,a 2-week washout period was undertaken during which the individualsmaintained their normal lifestyle and eating habits while avoiding alllycopene foods such as tomato products, guava, pink grapefruits and thelike. Third, at the end of the 2-week washout period, each individual'sserum was sampled (i.e., the first sample) after which, they wereassigned to one of the two study groups. Fourth, the individuals in eachgroup received their daily dosage for 12 consecutive weeks. Eachindividual was sampled after one week (i.e., the second sample), afterfour weeks (i.e., the third sample) and after twelve weeks (i.e., thefourth sample). Each serum sample was assayed to quantitativelydetermine therein the PSA, lycopene, creatine, bilirubin, alanine aminotransferase, hemoglobin, cholesterol, low-density lipoprotein,high-density lipoprotein, and testosterone levels. At each samplingtime, the test individuals were also responded to questions regardingtheir urinary functions taken from the International Prostate SymptomScore (IPSS) index developed and validated by a multidisciplinarymeasurement committee of the American Urological Association (Fowler etal., 1992, Journal of Urology 148:1549-57). The 7 questions comprisingthe IPSS questionnaire may be classified into 2 categories: questionsrelated to voiding or obstructive symptoms and questions related tostorage or irritative symptoms questions. Subject's IPSS scores wereused to evaluate the lower urinary tract symptoms (LUTS). Higher IPSSscores were indicative of individuals exhibiting a greater number ofsymptoms of LUTS.

The time “0” data (i.e., the first sample) are shown in Table 1.Individuals receiving a daily lycopene dose of 15 mg via one capsule ofa multi-carotenoids composition of the exemplary composition of thepresent invention showed a 2.6 times increase in their serum lycopenelevels, while individuals receiving a daily lycopene dose of 30 mg viatwo capsules of a multi-carotenoids composition daily showed a 3-foldincrease in their serum lycopene levels (Table 2).

TABLE 1 Summary of test individual baseline data at the first sampletime (0 time)* Multi-carotenoids compositions - Lycopene dosageParameter 15 mg/day 30 mg/day Age (years) 63.4 ± 8.1  63.9 ± 9.7  P =0.9 Median PSA (ng/mL) 8.8 ± 4.2 7.8 ± 3.8 P = 0.3 Median PSA range(ng/mL)  3.5-18.4  2.7-17.5 IPSS 11.3 ± 5.8  12.3 ± 6.5  P = 0.5 Bodymass index 24.6 ± 2.0  24.2 ± 2.9  P = 0.9 Serum total lycopene 297.9 ±127.3 303.0 ± 162.3 P = 0.9 (ng/mL) Serum creatine (mg/dL) 1.07 ± 0.151.14 ± 0.15 P = 0.06 Serum bilirubin (mg/dL) 0.9 ± 0.3 0.9 ± 0.3 P = 0.4Alanine amino transferase 21.6 ± 7.9  18.5 ± 6.3  P = 0.08 (U/L) Serumhemoglobin (mg/dL) 14.4 ± 1.0  14.6 ± 1.2  P = 0.5 Serum cholesterol(mg/dL) 198.4 ± 33.7  205.9 ± 32.5  P = 0.4 Low-density lipoprotein122.5 ± 28.2  132.1 ± 54.9  P = 0.4 (mg/dL) High-density lipoprotein41.5 ± 9.2  44.2 ± 10.3 P = 0.3 (mg/dL) Serum triglycerides 122.6 ±53.1  115.6 ± 68.4  P = 0.7 (mg/dL) Serum testosterone (mg/dL) 4.5 ± 1.74.8 ± 1.9 P = 0.5 *Data are means ± standard deviations

TABLE 2 Changes in serum lycopene levels after 12 weeks ofsupplementation with the exemplary composition of the presentinvention*. Multi-carotenoids compositions - Lycopene dosage Sample time15 mg/day 30 mg/day Time “0” (baseline) 279.9 ± 127.3 303.0 ± 162.3 P =0.9 After 12 weeks 780.0 ± 224.1 947.5 ± 290.4 P = 0.01 *Serum lycopenelevels are reported as ng./mL means ± standard deviations.

The median results indicated that the test individuals from both dailydosage groups showed marginal declines in their PSA levels over the12-week study (Table 3). However, a sub-group of 23 test individualswith baseline PSA levels greater than 8.0 at the first sampling time(i.e., time “0”), from both treatment groups, showed significantdecreases in their PSA levels over the 12-week study (Table 4).

TABLE 3 Changes in PSA levels during 12 weeks of supplementation withthe exemplary composition of the present invention*. Multi-carotenoidscompositions - Lycopene dosage Sample time 15 mg/day 30 mg/day Time “0”(baseline) 8.8 ± 4.2 7.8 ± 3.7 After 4 weeks 8.3 ± 3.9 7.0 ± 3.8 %change from baseline   −4%   −9% P = 0.08 P = 0.01 After 12 weeks 8.0 ±3.8 7.5 ± 4.0 % change from baseline −5.2% −3.1% P = 0.17 P = 0.22 *PSAdata are reported as ng/mL means ± standard deviations.

TABLE 4 Changes in PSA levels in test individuals with elevated baselinePSAs, during 12 weeks of supplementation with the exemplary compositionof the present invention. Sample time PSA level (ng/mL) Time “0”(baseline) 12.4 ± 3.2 After 4 weeks 11.2 ± 4.1 % change from baseline−11% P = 0.01 After 12 weeks 10.9 ± 4.0 % change from baseline −12% P =0.04

The test individuals from both daily dosage groups showed a progressivedecline in their IPSS indices over the 12-week study (Table 5).

TABLE 5 Changes in test individuals’ IPSS indices during 12 weeks ofsupplementation with the exemplary composition of the presentinvention*. Multi-carotenoids compositions - Lycopene dosage Sample time15 mg/day 30 mg/day Time “0” (baseline) 11.3 ± 5.8  12.3 ± 6.5  After 4weeks 9.5 ± 5.0 9.0 ± 5.0 % change from baseline −14% −24% P = 0.002 P <0.001 After 12 weeks 9.1 ± 5.9 7.5 ± 4.0 % change from baseline −17%−32% P = 0.012 P < 0.001 *IPSS data are reported as points means ±standard deviations.

Furthermore, the test individuals from both daily dosage groups showedprogressive declines in their obstructive IPSS scores and theirirritative IPSS scores over the 12-week study (Table 6).

TABLE 6 Changes in obstructive and irritative IPSS scores during 12weeks of supplementation with the exemplary composition of the presentinvention*. Multi-carotenoids compositions - Lycopene dosage Sample time15 mg/day 30 mg/day Obstructive IPSS Scores* Time “0” (baseline) 5.6 ±3.7 6.9 ± 4.8 After 4 weeks 4.7 ± 2.9 4.9 ± 3.5 % change from baseline−0.4% −22% P = 0.04 P < 0.001 After 12 weeks 4.7 ± 3.7 4.0 ± 3.7 %change from baseline −3.4% −27% P = 0.18 P < 0.001 Irritative IPSSScores* Time “0” (baseline) 5.7 ± 3.0 5.4 ± 2.9 After 4 weeks 4.9 ± 2.74.1 ± 2.2 % change from baseline  −11% −16% P = 0.009 P < 0.001 After 12weeks 4.4 ± 2.5 3.6 ± 2.0 % change from baseline  −16% −27% P = 0.001 P< 0.001 *Obstructive and irritative IPSS data are reported as scoremeans ± standard deviations.

Data from this clinical study indicated that administration of amulti-carotenoids composition demonstrated positive effects on patientsexhibiting urinary impairments. More specifically, the data suggestedthat the administration of a multi-carotenoids composition wasassociated with a significant decrease in IPSS and may improve LUTS,particularly LUTS that is suggestive of BPH in men.

EXAMPLE 2 Effects of a Multi-Carotenoids Composition on PatientsExhibiting Urinary Impairments

A 12-week phase III double-blind, randomized, placebo-controlled,parallel study was initiated with a group of eligible male subjects toassess the effects of a multi-carotenoids composition. Morespecifically, the clinical study evaluated the potential effects ofadministration of a multi-carotenoids composition on serum PSA levelsand LUTS. In particular, the study evaluated the potential effects ofadministration of a multi-carotenoids composition on benign prostatehypertrophy (BPH).

Individual subjects were divided into: (a) a first group of subjects whoreceived a daily oral dose of a multi-carotenoids composition therebyproviding a daily nutritional supplement of 30 mg of lycopene, and (b) asecond group of subjects who received a daily oral dose of a placebo,based on selected clinical parameters associated with prostate andurinary system health.

The inclusion and exclusion criteria for the trial were similar to thoseoutlined in Example 1 above.

The trial followed a general protocol of screening, evaluation andselection of the individuals for participating in the trial;administration of the daily supplements to the selected trial subjectsover the course of the trial; and collection data samples from each ofthe selected trial subjects.

The effects of administration of a multi-cartenoids composition on eachof the subjects were evaluated based on the data gathered and resultswere reviewed for the existence of a placebo effect. A placebo effect isthe measurable, observable, or felt improvement in health or behaviourthat is not attributable to a medication or invasive treatment that hasbeen administered.

The embodiments of the present invention comprising multi-carotenoidscompositions as disclosed herein for provision of a daily nutritionalsupplement and/or botanical drug of about 5 mg, at least about 10 mg, atleast about 15, and at least 30 mg of lycopene, are useful forameliorating the effects of aging-related impaired urinary functions inmen, for example BPH, LUTS, prostate cancer and the like.

While particular exemplary embodiments of the present invention havebeen described in the foregoing, it is to be understood that otherembodiments are possible within the scope of the present invention andare intended to be included herein. In view of numerous changes andvariations that will be apparent to persons skilled in the art, thescope of the present invention is to be considered limited solely by theappended claims.

1. A method for ameliorating the effects of aging-related urinary tractmalfunctions in men, said urinary tract malfunctions comprising thegroup of benign prostate hyperplasia and lower urinary tract symptoms,the method comprising orally administrating an effective amount of acomposition comprising: a tomato extract comprising about 2% to 10% byweight of lycopene, about 0.25% to 2% by weight of phytoene, and about0.2% to 2% by weight of phytofluene; an edible oil; and a suitablecarrier.
 2. A method for ameliorating the effects of aging-relatedurinary tract malfunctions in men, said urinary tract malfunctionscomprising the group of benign prostate hyperplasia and lower urinarytract symptoms, the method comprising orally administrating an effectiveamount of a composition comprising: a tomato extract comprising at leastlycopene, phytoene, and phytofluene; and a suitable carrier.
 3. A methodaccording to claim 1, wherein said tomato extract of said compositionadditionally comprises at least one carotene selected from the groupcomprising β-carotene, γ-carotene, and δ-carotene, a phytosterol, atocopheral and a phospholipid.
 4. A method according to claim 1, whereinsaid edible oil is selected from the group comprising soya oil, pumpkinseed oil, grape-seed oil and combinations thereof.
 5. A method accordingto claim 1, wherein said carrier is selected from the group comprisingsoft gel capsules, hard capsules, sachet packets, tablets, beverages andcombinations thereof.
 6. A method according to claim 1, wherein the oraladministration of said composition provides a daily nutritionalsupplement of about 5 mg lycopene.
 7. A method according to claim 1,wherein the oral administration of said supplement composition providesa daily nutritional supplement of at least about 10 mg lycopene.
 8. Amethod according to claim 1, wherein the oral administration of saidcomposition provides a daily nutritional supplement of at least about 15mg lycopene.
 9. A method according to claim 1, wherein the oraladministration of said composition provides a daily nutritionalsupplement of at least about 30 mg lycopene.
 10. A method according toclaim 1, wherein said tomato extract of said composition comprises about4% to 6% by weight of lycopene, about 0.4% to 0.6% by weight ofphytoene, and about 0.3% to 0.5% by weight of phytofluene.
 11. A methodaccording to claim 10, wherein said tomato extract of said compositionadditionally comprises at least one carotene selected from the groupcomprising β-carotene, γ-carotene, and δ-carotene, a phytosterol, atocopheral and a phospholipid.
 12. A method according to claim 1,wherein said tomato extract of said composition is further processedinto a formulation component selected from the group comprisingoleoresins, beadlets, dry powders, paste and combinations thereof.
 13. Amethod according to claim 12, wherein the oral administration of saidcomposition provides a daily nutritional supplement of about 5 mglycopene.
 14. A method according to claim 12, wherein the oraladministration of said composition provides a daily nutritionalsupplement of at least about 10 mg lycopene.
 15. A method according toclaim 12, wherein the oral administration of said composition provides adaily nutritional supplement of at least about 15 mg lycopene.
 16. Amethod according to claim 12, wherein the oral administration of saidcomposition provides a daily nutritional supplement of at least about 30mg lycopene.
 17. A method according to claim 1, wherein said tomatoextract of said composition comprises about 4% to 7% by weight oflycopene, about 0.4% to 0.7% by weight of phytoene; about 0.3% to 0.6%by weight of phytofluene, about 1% to 3% by weight of a tocopherol,about 1% to 2% by weight of a β-carotene, about 0.3% to 0.6% by weightof a phytosterol, about 5% to 10% by weight of a phospholipid.
 18. Amethod according to claim 17, wherein the oral administration of saidcomposition provides a daily nutritional supplement of about 5 mglycopene.
 19. A method according to claim 17, wherein the oraladministration of said composition provides a daily nutritionalsupplement of at least about 10 mg lycopene.
 20. A method according toclaim 17, wherein the oral administration of said composition provides adaily nutritional supplement of at least about 15 mg lycopene.
 21. Amethod according to claim 17, wherein the oral administration of saidcomposition provides a daily nutritional supplement of at least about 30mg lycopene.
 22. A method according to claim 17, wherein said edible oilis selected from the group comprising soya oil, pumpkin seed oil,grape-seed oil and combinations thereof.
 23. Use of a multi-carotenoidscomposition for the treatment of urinary tract malfunctions comprisingthe group of benign prostate hyperplasia and lower urinary tractsymptoms, wherein said composition comprises: a tomato extractcomprising about 2% to 10% by weight of lycopene, about 0.25% to 2% byweight of phytoene, and about 0.2% to 2% by weight of phytofluene; anedible oil; and a suitable carrier.
 24. A use according to claim 23,wherein said tomato extract of said composition comprises about 4% to 6%by weight of lycopene, about 0.4% to 0.6% by weight of phytoene, andabout 0.3% to 0.5% by weight of phytofluene.
 25. A use according toclaim 23, wherein said tomato extract of said composition additionallycomprises at least one carotene selected from the group comprisingβ-carotene, γ-carotene, and δ-carotene, a phytosterol, a tocopheral anda phospholipid.
 26. Use of a multi-carotenoids composition for treatmentof urinary tract malfunctions comprising the group of benign prostatehyperplasia and lower urinary tract symptoms, wherein said compositioncomprises: a tomato extract comprising about 4% to 7% by weight oflycopene, about 0.4% to 0.7% by weight of phytoene; about 0.3% to 0.6%by weight of phytofluene, about 1% to 3% by weight of a tocopherol,about 1% to 2% by weight of a β-carotene, about 0.3% to 0.6% by weightof a phytosterol, about 5% to 10% by weight of a phospholipid; an edibleoil; and a suitable carrier.